HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → Ethyl 2-(Benzylsulfanyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Acetic acid, (phenylthio)-, ethyl ester | HCID 97312 | — |
| Solvent | Sodium ethoxide | HCID 2723922 | — |
| Product | Ethyl 2-(Benzylsulfanyl)acetate | HCID 3344750 | — |
Reaction Steps
The procedure is as in Example 2 for the preparation of ethyl (phenylthio)acetate starting with ethyl bromoacetate (16.7 g), a 2M ethanolic solution of sodium ethylate (50 cc) and benzylmercaptan (11.7 cc). Ethyl (benzylthio)acetate (19.4 g) is thereby obtained, and is used in the crude state in the subsequent phases.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04971979 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-a9addfbf040a4d65af3dcbf5a9aa07ba |
| Source note | uspto-grants-1990_11 |